Pregled bibliografske jedinice broj: 673669
GENDER-SPECIFIC EFFECTS OF PPARG, APOE, ACE, LPL, IL-6 AND AT1R GENE VARIANTS ON METABOLIC SYNDROME
GENDER-SPECIFIC EFFECTS OF PPARG, APOE, ACE, LPL, IL-6 AND AT1R GENE VARIANTS ON METABOLIC SYNDROME // Biochemia Medica / Šimundić, Ana-Maria (ur.).
Zagreb: Medicinska naklada, 2012. str. A158-A159 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 673669 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
GENDER-SPECIFIC EFFECTS OF PPARG, APOE, ACE, LPL, IL-6 AND AT1R GENE VARIANTS ON METABOLIC SYNDROME
Autori
Božina, Tamara ; Sertić, Jadranka ; Lovrić, Jasna ; Jelaković, Bojan ; Merkler, Marijan ; Reiner, Željko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Biochemia Medica
/ Šimundić, Ana-Maria - Zagreb : Medicinska naklada, 2012, A158-A159
Skup
2nd European Joint Congress of EFLM and UEMS and 7th Congress of the Croatian Society for Medical Biochemistry and Laboratory medicine
Mjesto i datum
Dubrovnik, Hrvatska, 10.10.2012. - 13.10.2012
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
metabolic syndrome; gene variants
Sažetak
Background. Metabolic syndrome (MS) is a cluster of modifiable risk factors including hypertension, abdominal obesity, dyslipidemia and insulin resistance, associated with nonmodifiable risk factors, such as age, sex and genetic background. We investigated the possible role of gene polymorphisms of PPARG (Pro12Ala), ApoE (ε2, ε3, ε4), LPL (P+/-), IL-6 (-174G>C), ACE (I/D) and AT1R (1166A>C) in MS. Methods. 516 individuals were investigated including 263 patients with MS and 253 subjects without MS criteria. Genotyping was performed using PCR based methods. Results. In female group associations were found for: LPL and ACE with MS (p=0.04) ; PPARG and LPL with blood pressure, (p=0.04) ; LPL with cholesterol and LDL (p=0.01 and p=0.05, respectively). Significant gene interactions observed between: APOE and PPARG, ACE and APOE were associated with BMI (p=0.01 and p=0.05, respectively) ; LPL and PPARG were associated with triglycerides (p=0.03). For males we found associations of: LPL variants with MS (p=0.02), BMI (p=0.002) and waist circumference (p=0.008) ; PPARG and APOE with BMI (p=0.05) ; IL-6 with CRP (p=0.02). Significant gene interactions observed between: PPARG and AT1R were associated with blood pressure (p=0.05) ; PPARG and APOE with triglycerides (p=0.02) ; PPARG and APOE, PPARG and IL6 (p=0.03), ACE and APOE (p=0.0002) with cholesterol ; PPARG and LPL (p=0.003), PPARG and IL6 (p=0.06) with HDL ; PPARG and IL6 (p=0.01), ACE and APOE (p=0.04) ; PPARG and APOE, LPL and ACE (p=0.01), AT1R and ACE (p=0.06) with CRP. Conclusion. Gene variants of PPARG, APOE, LPL, ACE, AT1R and IL-6 could be susceptibility factors of obesity, lipid status, and glucose intolerance.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
108-1080134-0136 - Funkcijska genomika i proteomika rizičnih čimbenika ateroskleroze (Sertić, Jadranka, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Bojan Jelaković
(autor)
Jasna Lovrić
(autor)
Marijan Merkler
(autor)
Željko Reiner
(autor)
Tamara Božina
(autor)
Jadranka Sertić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE